FOXD1-dependent MICU1 expression regulates mitochondrial activity and cell differentiation

Santhanam Shanmughapriya; Dhanendra Tomar; Zhiwei Dong; Katherine J. Slovik; Neeharika Nemani; Kalimuthusamy Natarajaseenivasan; Edmund Carvalho; Christy Lu; Kaitlyn Corrigan; Venkata Naga Srikanth Garikipati; Jessica Ibetti; Sudarsan Rajan; Carlos Barrero; Kurt Chuprun; Raj Kishore; Salim Merali; Ying Tian; Wenli Yang; Muniswamy Madesh

doi:10.1038/s41467-018-05856-4

FOXD1-dependent MICU1 expression regulates mitochondrial activity and cell differentiation

Santhanam Shanmughapriya, Dhanendra Tomar, Zhiwei Dong, Katherine J. Slovik, Neeharika Nemani, Kalimuthusamy Natarajaseenivasan, Edmund Carvalho, Christy Lu, Kaitlyn Corrigan, Venkata Naga Srikanth Garikipati, Jessica Ibetti, Sudarsan Rajan, Carlos Barrero, Kurt Chuprun, Raj Kishore, Salim Merali, Ying Tian, Wenli Yang, Muniswamy Madesh

Division of Cardiology

Producción científica: Article › revisión exhaustiva

33 Citas (Scopus)

Resumen

Although many factors contribute to cellular differentiation, the role of mitochondria Ca²⁺ dynamics during development remains unexplored. Because mammalian embryonic epiblasts reside in a hypoxic environment, we intended to understand whether _mCa²⁺ and its transport machineries are regulated during hypoxia. Tissues from multiple organs of developing mouse embryo evidenced a suppression of MICU1 expression with nominal changes on other MCU complex components. As surrogate models, we here utilized human embryonic stem cells (hESCs)/induced pluripotent stem cells (hiPSCs) and primary neonatal myocytes to delineate the mechanisms that control _mCa²⁺ and bioenergetics during development. Analysis of MICU1 expression in hESCs/hiPSCs showed low abundance of MICU1 due to its direct repression by Foxd1. Experimentally, restoration of MICU1 established the periodic _cCa²⁺ oscillations and promoted cellular differentiation and maturation. These findings establish a role of _mCa²⁺ dynamics in regulation of cellular differentiation and reveal a molecular mechanism underlying this contribution through differential regulation of MICU1.

Idioma original	English (US)
Número de artículo	3449
Publicación	Nature communications
Volumen	9
N.º	1
DOI	https://doi.org/10.1038/s41467-018-05856-4
Estado	Published - dic 1 2018

ASJC Scopus subject areas

General Chemistry
General Biochemistry, Genetics and Molecular Biology
General Physics and Astronomy

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10.1038/s41467-018-05856-4

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Shanmughapriya, S., Tomar, D., Dong, Z., Slovik, K. J., Nemani, N., Natarajaseenivasan, K., Carvalho, E., Lu, C., Corrigan, K., Garikipati, V. N. S., Ibetti, J., Rajan, S., Barrero, C., Chuprun, K., Kishore, R., Merali, S., Tian, Y., Yang, W., & Madesh, M. (2018). FOXD1-dependent MICU1 expression regulates mitochondrial activity and cell differentiation. Nature communications, 9(1), Artículo 3449. https://doi.org/10.1038/s41467-018-05856-4

Shanmughapriya, S, Tomar, D, Dong, Z, Slovik, KJ, Nemani, N, Natarajaseenivasan, K, Carvalho, E, Lu, C, Corrigan, K, Garikipati, VNS, Ibetti, J, Rajan, S, Barrero, C, Chuprun, K, Kishore, R, Merali, S, Tian, Y, Yang, W & Madesh, M 2018, 'FOXD1-dependent MICU1 expression regulates mitochondrial activity and cell differentiation', Nature communications, vol. 9, n.º 1, 3449. https://doi.org/10.1038/s41467-018-05856-4

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abstract = "Although many factors contribute to cellular differentiation, the role of mitochondria Ca2+ dynamics during development remains unexplored. Because mammalian embryonic epiblasts reside in a hypoxic environment, we intended to understand whether mCa2+ and its transport machineries are regulated during hypoxia. Tissues from multiple organs of developing mouse embryo evidenced a suppression of MICU1 expression with nominal changes on other MCU complex components. As surrogate models, we here utilized human embryonic stem cells (hESCs)/induced pluripotent stem cells (hiPSCs) and primary neonatal myocytes to delineate the mechanisms that control mCa2+ and bioenergetics during development. Analysis of MICU1 expression in hESCs/hiPSCs showed low abundance of MICU1 due to its direct repression by Foxd1. Experimentally, restoration of MICU1 established the periodic cCa2+ oscillations and promoted cellular differentiation and maturation. These findings establish a role of mCa2+ dynamics in regulation of cellular differentiation and reveal a molecular mechanism underlying this contribution through differential regulation of MICU1.",

author = "Santhanam Shanmughapriya and Dhanendra Tomar and Zhiwei Dong and Slovik, {Katherine J.} and Neeharika Nemani and Kalimuthusamy Natarajaseenivasan and Edmund Carvalho and Christy Lu and Kaitlyn Corrigan and Garikipati, {Venkata Naga Srikanth} and Jessica Ibetti and Sudarsan Rajan and Carlos Barrero and Kurt Chuprun and Raj Kishore and Salim Merali and Ying Tian and Wenli Yang and Muniswamy Madesh",

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AU - Shanmughapriya, Santhanam

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AU - Dong, Zhiwei

AU - Slovik, Katherine J.

AU - Nemani, Neeharika

AU - Natarajaseenivasan, Kalimuthusamy

AU - Carvalho, Edmund

AU - Lu, Christy

AU - Corrigan, Kaitlyn

AU - Garikipati, Venkata Naga Srikanth

AU - Ibetti, Jessica

AU - Rajan, Sudarsan

AU - Barrero, Carlos

AU - Chuprun, Kurt

AU - Kishore, Raj

AU - Merali, Salim

AU - Tian, Ying

AU - Yang, Wenli

AU - Madesh, Muniswamy

PY - 2018/12/1

Y1 - 2018/12/1

N2 - Although many factors contribute to cellular differentiation, the role of mitochondria Ca2+ dynamics during development remains unexplored. Because mammalian embryonic epiblasts reside in a hypoxic environment, we intended to understand whether mCa2+ and its transport machineries are regulated during hypoxia. Tissues from multiple organs of developing mouse embryo evidenced a suppression of MICU1 expression with nominal changes on other MCU complex components. As surrogate models, we here utilized human embryonic stem cells (hESCs)/induced pluripotent stem cells (hiPSCs) and primary neonatal myocytes to delineate the mechanisms that control mCa2+ and bioenergetics during development. Analysis of MICU1 expression in hESCs/hiPSCs showed low abundance of MICU1 due to its direct repression by Foxd1. Experimentally, restoration of MICU1 established the periodic cCa2+ oscillations and promoted cellular differentiation and maturation. These findings establish a role of mCa2+ dynamics in regulation of cellular differentiation and reveal a molecular mechanism underlying this contribution through differential regulation of MICU1.

AB - Although many factors contribute to cellular differentiation, the role of mitochondria Ca2+ dynamics during development remains unexplored. Because mammalian embryonic epiblasts reside in a hypoxic environment, we intended to understand whether mCa2+ and its transport machineries are regulated during hypoxia. Tissues from multiple organs of developing mouse embryo evidenced a suppression of MICU1 expression with nominal changes on other MCU complex components. As surrogate models, we here utilized human embryonic stem cells (hESCs)/induced pluripotent stem cells (hiPSCs) and primary neonatal myocytes to delineate the mechanisms that control mCa2+ and bioenergetics during development. Analysis of MICU1 expression in hESCs/hiPSCs showed low abundance of MICU1 due to its direct repression by Foxd1. Experimentally, restoration of MICU1 established the periodic cCa2+ oscillations and promoted cellular differentiation and maturation. These findings establish a role of mCa2+ dynamics in regulation of cellular differentiation and reveal a molecular mechanism underlying this contribution through differential regulation of MICU1.

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FOXD1-dependent MICU1 expression regulates mitochondrial activity and cell differentiation

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